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10.4103/0971-4065.161021

http://scihub22266oqcxt.onion/10.4103/0971-4065.161021
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C4795432!4795432!27051141
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suck abstract from ncbi


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pmid27051141      Indian+J+Nephrol 2016 ; 26 (2): 142-4
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  • Eosinophilic granulomatosis with polyangiitis with severe pulmonary hemorrhage treated with rituximab #MMPMID27051141
  • Baikunje S; Vankalakunti M; Upadhyaya VS; Hosmane GB
  • Indian J Nephrol 2016[Mar]; 26 (2): 142-4 PMID27051141show ga
  • Eosinophilic granulomatosis with polyangiitis (EGPA) is characterized by systemic vasculitis, asthma and eosinophilia. Severe pulmonary hemorrhage is rare. Renal involvement is seen in approximately 25% and can vary from isolated urinary abnormality to rapidly progressive glomerulonephritis. There is limited evidence to support the use of rituximab in this condition. We present a patient with EGPA who had severe pulmonary hemorrhage and rapidly progressive glomerulonephritis. He responded to standard treatment including prednisolone, cyclophosphamide, and plasma exchange. He subsequently had a relapse of pulmonary hemorrhage that was treated successfully with rituximab.
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